题名 | Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in mice |
作者 | |
发表日期 | 2024-05-21 |
发表期刊 | Biochemical and biophysical research communications 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Journal Article |
关键词 | Hyperuricemia Rdh12 Uric acid |
其他关键词 | GENE ; GOUT ; VARIANT ; URATE ; DISRUPTION ; REDUCTION ; DYSTROPHY |
摘要 | Hyperuricemia is a chronic metabolic disease caused by purine metabolism disorder. And several gene loci and transporter proteins that associated with uric acid transport functions have been identified. Retinol Dehydrogenase 12 (RDH12), recognized for its role in safeguarding photoreceptors, and our study investigated the potential impact of Rdh12 mutations on other organs and diseases, particularly hyperuricemia. We assessed Rdh12 mRNA expression levels in various tissues and conducted serum biochemical analyses in Rdh12-/- mice. Compared with the wild type, significant alterations in serum uric acid levels and kidney-related biochemical indicators have been revealed. Then further analysis, including quantitative RT-PCR of gene expression in the liver and kidney, highlighted variations in the expression levels of specific genes linked to hyperuricemia. And renal histology assessment exposed mild pathological lesions in the kidneys of Rdh12-/- mice. In summary, our study suggests that Rdh12 mutations impact not only retinal function but also contribute to hyperuricemia and renal disease phenotypes in mice. Our finding implies that individuals with Rdh12 mutations may be prone to hyperuricemia and gout, emphasizing the significance of preventive measures and regular examinations in daily life |
出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
ISSN | 0006-291X |
EISSN | 1090-2104 |
卷号 | 709 |
DOI | 10.1016/j.bbrc.2024.149809 |
页数 | 6 |
WOS类目 | Biochemistry & Molecular Biology ; Biophysics |
WOS研究方向 | Biochemistry & Molecular Biology ; Biophysics |
WOS记录号 | WOS:001224367400001 |
收录类别 | PUBMED ; SCOPUS ; SCIE |
URL | 查看原文 |
PubMed ID | 38552555 |
SCOPUSEID | 2-s2.0-85188929251 |
通讯作者地址 | [Pan, Qing]Department of Ophthalmology,Zhejiang University Medical School 1st Affiliated Hospital,79 Qingchun Road,Hangzhou,China ; [Qi, Ming]Department of Cell Biology and Medical Genetics,School of Medicine Zhejiang University,Research Building A713, Yuhangtang Road 866,Hangzhou,China |
Scopus学科分类 | Biophysics;Biochemistry;Molecular Biology;Cell Biology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/211056 |
专题 | 附属第一医院_生殖医学中心 |
通讯作者 | Qi, Ming; Pan, Qing |
作者单位 | 1.Department of Ophthalmology,Zhejiang University Medical School First Affiliated Hospital,Hangzhou,310000,China; 2.Department of Cell Biology and Medical Genetics,School of Medicine Zhejiang University,Hangzhou,310000,China; 3.Reproductive Medicine Center,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China; 4.Center for Reproductive Medicine,Department of Reproductive Endocrinology,Zhejiang Provincial People's Hospital(Affiliated People's Hospital,Hangzhou Medical College),Zhejiang,Hangzhou,310000,China; 5.Assisted Reproduction Unit,Department of Obstetrics and Gynecology,Department of Laboratory Medicine,Sir Run Run Shaw Hospital,Zhejiang University School of Medicine,Key Laboratory of Reproductive Dysfunction Management of Zhejiang Province,Hangzhou,310000,China; 6.DIAN Diagnostics,Hangzhou,310000,China; 7.Department of Pathology and Laboratory of Medicine,University of Rochester Medical Centre,NY,Rochester,14609,United States; 8.HVP-China,Hangzhou,310000,China |
推荐引用方式 GB/T 7714 | Bian, Jiaxin,Chen, Hongyu,Sun, Junhui,et al. Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in mice[J]. Biochemical and biophysical research communications,2024,709. |
APA | Bian, Jiaxin, Chen, Hongyu, Sun, Junhui, Han, Shuai, Qi, Ming, & Pan, Qing. (2024). Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in mice. Biochemical and biophysical research communications, 709. |
MLA | Bian, Jiaxin,et al."Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in mice".Biochemical and biophysical research communications 709(2024). |
条目包含的文件 | 条目无相关文件。 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论